Does SPARSENTAN Cause Adverse event? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Adverse event have been filed in association with SPARSENTAN (FILSPARI). This represents 0.5% of all adverse event reports for SPARSENTAN.
16
Reports of Adverse event with SPARSENTAN
0.5%
of all SPARSENTAN reports
0
Deaths
2
Hospitalizations
How Dangerous Is Adverse event From SPARSENTAN?
Of the 16 reports, 2 (12.5%) required hospitalization.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SPARSENTAN. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does SPARSENTAN Cause?
Dizziness (521)
Fatigue (448)
Hypotension (377)
Product use in unapproved indication (262)
Nausea (231)
Peripheral swelling (197)
Headache (186)
Pruritus (171)
Blood creatinine increased (145)
Glomerular filtration rate decreased (141)
What Other Drugs Cause Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which SPARSENTAN Alternatives Have Lower Adverse event Risk?
SPARSENTAN vs SPESOLIMAB-SBZO
SPARSENTAN vs SPIRAMYCIN
SPARSENTAN vs SPIRIVA
SPARSENTAN vs SPIRONOLACTONE
SPARSENTAN vs SPRYCEL